A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624939



Internal ID7011789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130541074..130566230hg38UCSC Ensembl
chr10:132339338..132364494hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3825157
hg1925157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13975582, essv13975585, essv13975584, essv13975581, essv13975583
SamplesHG03449, HG03926, NA19663, HG01390, NA19661
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624939
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer